dc.contributor.author | Kalogirou, Andreas S. | en |
dc.contributor.author | Koutentis, Panayiotis A. | en |
dc.creator | Kalogirou, Andreas S. | en |
dc.creator | Koutentis, Panayiotis A. | en |
dc.date.accessioned | 2021-01-25T09:44:46Z | |
dc.date.available | 2021-01-25T09:44:46Z | |
dc.date.issued | 2018 | |
dc.identifier.issn | 0040-4039 | |
dc.identifier.uri | http://gnosis.library.ucy.ac.cy/handle/7/63016 | |
dc.description.abstract | The Buchwald-Hartwig Pd-catalyzed C-N coupling reaction of 5-substituted 3-chloro-4H-1,2,6-thiadiazin-4-ones with primary (het)arylamines is described, affording twenty new 3,5-disubstituted 4H-1,2,6-thiadiazin-4-ones in 56–99% yield. The protocol enables the mild preparation of difficult to access 3,5-dianilino-1,2,6-4H-thiadiazin-4-ones. The reaction scope and limitations are discussed. | en |
dc.language.iso | en | en |
dc.source | Tetrahedron Letters | en |
dc.source.uri | http://www.sciencedirect.com/science/article/pii/S0040403918306932 | |
dc.title | Pd-catalyzed C-N coupling of primary (het)arylamines with 5-substituted 3-chloro-4H-1,2,6-thiadiazin-4-ones | en |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | 10.1016/j.tetlet.2018.05.068 | |
dc.description.volume | 59 | |
dc.description.issue | 27 | |
dc.description.startingpage | 2653 | |
dc.description.endingpage | 2656 | |
dc.author.faculty | 002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences | |
dc.author.department | Τμήμα Χημείας / Department of Chemistry | |
dc.type.uhtype | Article | en |
dc.source.abbreviation | Tetrahedron Letters | en |
dc.contributor.orcid | Kalogirou, Andreas S. [0000-0002-5476-5805] | |
dc.contributor.orcid | Koutentis, Panayiotis A. [0000-0002-4652-7567] | |
dc.gnosis.orcid | 0000-0002-5476-5805 | |
dc.gnosis.orcid | 0000-0002-4652-7567 | |